A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6606248



Internal ID20979319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:150922690..150946195hg38UCSC Ensembl
chr6:151243826..151267331hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg3823506
hg1923506
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18141056
Samples
Known GenesMTHFD1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6606248
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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